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绘制小鼠行为性状的数量性状基因座图谱。

Mapping quantitative trait loci for behavioral traits in the mouse.

作者信息

Johnson T E, DeFries J C, Markel P D

机构信息

Institute for Behavioral Genetics, University of Colorado, Boulder 80309.

出版信息

Behav Genet. 1992 Nov;22(6):635-53. doi: 10.1007/BF01066635.

Abstract

After many years of studying various behavioral characters in the mouse, it is clear that most are heritable and are specified by complexes of genes or quantitative trait loci (QTLs). In order to attain a more complete understanding of the genetic causes of individual differences in behavior, the mechanism of action of these QTLs must be elucidated. The most straightforward approach to determining the mechanism of action of a particular QTL is to identify and molecularly clone the gene; this can be done by positional cloning, which depends on precise knowledge of the genetic map position. As the genetic data base for the mouse genome continues to develop, such strategies will become increasingly easy to perform. Here we suggest a multistage strategy for QTL mapping using recombinant-inbred strains of mice: (1) characterize genomic DNA from parental strains originally used to generate the RI strains; (2) characterize the RI strains for a quantitative character and for DNA markers that differ in the parental strains; and (3) assess the quantitative character in F2 mice derived from crosses between the parental strains, then determine the genotypes of extreme F2 mice for markers that account for at least 5% of the additive genetic variance. Data from these F2 crosses can be used to test hypotheses from the analysis of RI strains, i.e., that a QTL maps to a particular region. Using data from the mouse genome data base, this strategy should allow the molecular identification of the gene based on a candidate-gene approach. We illustrate the approach with examples from our work in mapping QTLs specifying neural sensitivity to the anesthetic effects of ethanol.

摘要

经过多年对小鼠各种行为特征的研究,很明显大多数行为特征是可遗传的,并且由基因复合体或数量性状位点(QTL)决定。为了更全面地了解行为个体差异的遗传原因,必须阐明这些QTL的作用机制。确定特定QTL作用机制的最直接方法是鉴定并对该基因进行分子克隆;这可以通过定位克隆来完成,而定位克隆依赖于对遗传图谱位置的精确了解。随着小鼠基因组遗传数据库的不断发展,此类策略将变得越来越容易实施。在此,我们提出一种使用重组近交系小鼠进行QTL定位的多阶段策略:(1)对最初用于产生RI品系的亲本品系的基因组DNA进行特征分析;(2)对RI品系的一个数量性状以及亲本品系中存在差异的DNA标记进行特征分析;(3)评估源自亲本品系杂交的F2小鼠的数量性状,然后确定极端F2小鼠对于占加性遗传方差至少5%的标记的基因型。来自这些F2杂交的数据可用于检验基于RI品系分析得出的假设,即某个QTL定位于特定区域。利用小鼠基因组数据库中的数据,该策略应能基于候选基因方法对基因进行分子鉴定。我们用我们在定位决定对乙醇麻醉作用神经敏感性的QTL的工作中的实例来说明该方法。

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